The purpose of this study is to evaluate the safety, tolerability and efficacy of V117957 in subjects with interstitial cystitis/bladder pain syndrome, compared to placebo.



Eligible Ages
Over 18 Years
Eligible Genders
Accepts Healthy Volunteers

Inclusion Criteria

include: 1. Female, age ≥18 years and capable of voiding independently. Able to comply with acceptable methods of contraception. 2. Diagnosis of IC/BPS or meets criteria for IC/BPS as defined by the American Urology Association as "an unpleasant sensation (pain, pressure, discomfort) perceived to be related to the urinary bladder, associated with lower urinary tract symptoms for more than six weeks duration, in the absence of infection or other identifiable causes". 3. Subject has Bladder Pain/Interstitial Cystitis Symptom Scale (BPIC-SS) total score of ≥19 and worst bladder pain/discomfort sub-score of ≥4 to ≤9. 4. Has undergone evaluation to rule out other conditions that cause bladder pain/discomfort. Any microscopic or gross hematuria that has not been evaluated in the past 12 months will require appropriate clinical evaluation to determine study eligibility.

Exclusion Criteria

include: 1. Pelvic floor tenderness in the absence of bladder tenderness on physical examination by primary investigator. 2. Urinary tract infection (UTI) within the past 30 days, or history of recurrent UTI. 3. Hematuria determined to be associated with bladder malignancy or other significant pathology. 4. Had surgical procedure at any time that affected bladder function. 5. Received intravesical therapy or had bladder hydrodistension, fulguration, botulinum toxin, or triamcinolone bladder injection, percutaneous nerve stimulation. A subject receiving such treatment(s) prior to screening is eligible if in the opinion of the investigator the procedure/ treatment resulted in no notable or enduring effect and subject continues to exhibit stable symptomology. 6. Has current or history of clinically significant kidney disease or abnormal kidney function, or nephrolithiasis. Other protocol-specific inclusion and exclusion criteria may apply.

Study Design

Phase 1
Study Type
Intervention Model
Crossover Assignment
Primary Purpose
Triple (Participant, Investigator, Outcomes Assessor)

Arm Groups

ArmDescriptionAssigned Intervention
  • Drug: V117957
    V117957 1 mg - 1 tablet taken orally at bedtime.
Placebo Comparator
  • Drug: Placebo
    Placebo to match V117957 tablets - 1 tablet taken orally at bedtime.

Recruiting Locations

MetroHealth System
Cleveland, Ohio 44109
Central Contact

More Details

Imbrium Therapeutics

Study Contact

Medical Services


Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.